Canonical Allele Identifier: CA375684170

Gene: ABO

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255812T>A , CM000671.2:g.133255812T>A	GRCh38
NC_000009.11:g.136131199T>A , CM000671.1:g.136131199T>A	GRCh37
NC_000009.10:g.135121020T>A	NCBI36
NG_006669.1:g.21856A>T
NG_006669.2:g.24404A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.948A>T
ENST00000647353.1:n.54-4660A>T
ENST00000679909.1:c.28+19350A>T	ENSP00000506089.1:n.28+19350A>T
ENST00000453660.3:n.930A>T
ENST00000538324.2:c.916A>T	ENSP00000483018.1:p.Asn306Tyr
ENST00000611156.4:c.916A>T	ENSP00000483265.1:p.Asn306Tyr
NM_020469.2:c.919A>T	NP_065202.2:p.Asn307Tyr
NM_020469.3:c.919A>T	NP_065202.2:p.Asn307Tyr